Canonical Allele Identifier: CA475509296

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257906T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490435T>C , CM000673.2:g.67490435T>C	GRCh38
NC_000011.9:g.67257906T>C , CM000673.1:g.67257906T>C	GRCh37
NC_000011.8:g.67014482T>C	NCBI36
NG_008969.1:g.12402T>C , LRG_460:g.12402T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.742T>C
ENST00000528641.7:c.576T>C	ENSP00000434982.3:p.Ser192=
ENST00000529797.2:n.1277T>C
ENST00000682324.1:c.469-562T>C	ENSP00000508017.1:n.469-562T>C
ENST00000682659.1:c.396T>C	ENSP00000507351.1:p.Ser132=
ENST00000682699.1:c.765T>C	ENSP00000507935.1:p.Ser255=
ENST00000683237.1:c.765T>C	ENSP00000507343.1:p.Ser255=
ENST00000683856.1:c.588T>C	ENSP00000507979.1:p.Ser196=
ENST00000684006.1:c.765T>C	ENSP00000507269.1:p.Ser255=
ENST00000684657.1:c.585T>C	ENSP00000507961.1:p.Ser195=
ENST00000279146.8:c.765T>C MANE Select	ENSP00000279146.3:p.Ser255=
ENST00000279146.7:c.765T>C	ENSP00000279146.3:p.Ser255=
ENST00000525341.1:c.417T>C	ENSP00000476993.1:p.Ser139=
ENST00000528641.6:c.576T>C	ENSP00000434982.2:p.Ser192=
NM_001302959.1:c.588T>C	NP_001289888.1:p.Ser196=
NM_001302960.1:c.765T>C	NP_001289889.1:p.Ser255=
NM_003977.3:c.765T>C	NP_003968.3:p.Ser255=
XM_024448761.1:c.765T>C	XP_024304529.1:p.Ser255=
NM_003977.4:c.765T>C MANE Select	NP_003968.3:p.Ser255=
NM_001302960.2:c.765T>C	NP_001289889.1:p.Ser255=
NM_001302959.2:c.588T>C	NP_001289888.1:p.Ser196=